Ciprofloxacin
- Product NDC
- 55154-5376
- 11-digit product format
- 551545376
- Labeler code
- 55154
- Product ID
- 55154-5376_7ac6eab1-313b-484e-8a10-e043df953076
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA075817
- Marketing category
- ANDA
- Marketing start
- 2012-06-29
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record